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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 50102Generated: October 25, 2026

Toluene → HCID 178500902, compound

https://huagongshe.com/reaction/50102

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
Reactant4-FluorobenzonitrileHCID 14517—
ReactantTin tetrachlorideHCID 24287—
ReactantMethyl 4-methyl-3-oxopentanoateHCID 2759969—
SolventHexaneHCID 8058—
ProductHCID 178500902HCID 17850090275.2%

Reaction Conditions

Temperature80 °C

Reaction Steps

75.09 g of methyl isobutyrylacetate (0.50 mol, concentration 96%) and 61.80 g of 4-fluorobenzonitrile (0.50 mol, concentration 98%) were introduced into [500 ml of toluene and treated with 144.7 g of tin tetrachloride (0.55 mol, concentration 99%) at room temperature over the course of 16 min. After half an hour at room temperature, the thick suspension was heated to 80° C. After. 3 h, 175 ml of toluene were distilled off at normal pressure, and the mixture was cooled to room temperature and treated with 450 ml of saturated sodium carbonate and 300 ml of ethyl acetate. The organic phase was separated off and the aqueous phase (after dilution with 300 ml of water) was again extracted with 300 ml of ethyl acetate. After drying the combined organic phases over sodium sulphate, the solvent was removed in vacuo (40° C./25 mbar). 127.2 g of crude product were obtained in the form of a slightly yellowish solid, which was dissolved in 160 ml of n-hexane (slightly turbid solution). After hot filtration and subsequent cooling in an ice bath, 99.8 g of methyl 2-[1-amino-1-(4-fluorophenyl)-methylene]-4-methyl-3-oxopentanoate were obtained after filtration in the form of a pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06710178B2
Source datasetuspto-grants-2004_03
ORD IDord-1f1b485b281146ec8dd6dd9e597da9cf
Source noteuspto-grants-2004_03